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Merck
CN

55472

N-Succinimidyl N-(2,4-dinitrophenyl)-6-aminocaproate

≥95% (HPLC)

Synonym(s):

N-(2,4-Dinitrophenyl)-6-aminocaproic acid N-succinimidyl ester, N-(2,4-Dinitrophenyl)-6-aminohexanoic acid N-succinimidyl ester

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About This Item

Empirical Formula (Hill Notation):
C16H18N4O8
CAS Number:
Molecular Weight:
394.34
NACRES:
NA.25
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
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Product Name

N-Succinimidyl N-(2,4-dinitrophenyl)-6-aminocaproate, ≥95% (HPLC)

InChI

1S/C16H18N4O8/c21-14-7-8-15(22)18(14)28-16(23)4-2-1-3-9-17-12-6-5-11(19(24)25)10-13(12)20(26)27/h5-6,10,17H,1-4,7-9H2

SMILES string

[O-][N+](=O)c1ccc(NCCCCCC(=O)ON2C(=O)CCC2=O)c(c1)[N+]([O-])=O

InChI key

IYBNUJCDIAGXNX-UHFFFAOYSA-N

assay

≥95% (HPLC)

storage temp.

−20°C

Quality Level

Application

N-(2,4-Dinitrophenyl)-6-aminocaproic acid N-succinimidyl ester is an amine-reactive DNP-X succinimidyl ester that may be used to create bioconjugates that may be detected with anti-dinitrophenyl (anti-DNP) antibodies.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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G H Keller et al.
Analytical biochemistry, 177(2), 392-395 (1989-03-01)
A photoactivatable reagent for introducing haptens onto DNA probes has been prepared using a commercially available bifunctional linker arm reagent and amino-derivatized 2,4-dinitrophenyl (DNP). The resulting compound (photo-DNP) couples efficiently to DNA using an ordinary sunlamp. Under optimum conditions, about

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